US8912274B2 - Water-dispersible varnish - Google Patents
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- US8912274B2 US8912274B2 US13/388,910 US200913388910A US8912274B2 US 8912274 B2 US8912274 B2 US 8912274B2 US 200913388910 A US200913388910 A US 200913388910A US 8912274 B2 US8912274 B2 US 8912274B2
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- 0 C1=CC=CC=C1.C1=CC=CC=C1.[1*]C(=C)C(=O)OCC([H])(O)COC.[2*]C([3*])(C)C.[4*]OC Chemical compound C1=CC=CC=C1.C1=CC=CC=C1.[1*]C(=C)C(=O)OCC([H])(O)COC.[2*]C([3*])(C)C.[4*]OC 0.000 description 18
- BOPOTZPAIYDONO-UHFFFAOYSA-N C1=CC=CC=C1.C=CCOC(C)=O.CC(C)=O Chemical compound C1=CC=CC=C1.C=CCOC(C)=O.CC(C)=O BOPOTZPAIYDONO-UHFFFAOYSA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
-
- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02K—DYNAMO-ELECTRIC MACHINES
- H02K3/00—Details of windings
- H02K3/30—Windings characterised by the insulating material
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/10—Esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
- C08F290/06—Polymers provided for in subclass C08G
- C08F290/064—Polymers containing more than one epoxy group per molecule
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F299/00—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
- C08F299/02—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/14—Polycondensates modified by chemical after-treatment
- C08G59/1433—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds
- C08G59/1438—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds containing oxygen
- C08G59/1455—Monocarboxylic acids, anhydrides, halides, or low-molecular-weight esters thereof
- C08G59/1461—Unsaturated monoacids
- C08G59/1466—Acrylic or methacrylic acids
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/14—Polycondensates modified by chemical after-treatment
- C08G59/1494—Polycondensates modified by chemical after-treatment followed by a further chemical treatment thereof
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
- C08L63/10—Epoxy resins modified by unsaturated compounds
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/062—Copolymers with monomers not covered by C09D133/06
- C09D133/068—Copolymers with monomers not covered by C09D133/06 containing glycidyl groups
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
- C09D151/08—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25B—REFRIGERATION MACHINES, PLANTS OR SYSTEMS; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS
- F25B1/00—Compression machines, plants or systems with non-reversible cycle
Definitions
- the present invention relates to water-dispersible varnish, an electric compressor using the water-dispersible varnish and a method of manufacturing the electric compressor, and a refrigeration and air-conditioning apparatus equipped with the electric compressor.
- FIG. 1 is a schematic explanatory diagram (schematic diagram of a longitudinal section) illustrating an embodiment of an electric compressor mounted on a refrigeration and air-conditioning apparatus.
- FIG. 2 is a partial schematic explanatory diagram illustrating a stator of a motor component in FIG. 1 , in which FIG. 1A is a plan view and FIG. 1B is a side view partially showing a cross sectional view. Note that in FIGS. 1 and 2 , a hermetic electric compressor is shown as an embodiment of an electric compressor mounted on a refrigeration and air-conditioning apparatus.
- a motor component 2 , a compression component 3 that is driven by the motor component 2 , and other components are provided in a hermetic vessel 1 . Further, refrigerating machine oil 4 is retained in the bottom portion of the hermetic vessel 1 .
- the motor component 2 includes a stator 21 and a rotor 22 .
- An outer circumference of the stator 21 is fixed to the hermetic vessel 1 .
- a magnet wire 6 provided in the stator 21 is connected to a sealed power terminal 7 provided in the hermetic vessel 1 , and is supplied with power from a power source (not shown).
- the rotor 22 is supported so as to maintain a constant gap with an inner circumference of the stator 21 , and is connected to the compression component 3 with the crankshaft 5 .
- the stator 21 includes a core 8 , the magnet wire 6 , an insulating film 10 , and a binding thread 11 .
- the core 8 is a cylindrical laminate of iron plates.
- the magnet wire 6 is arranged so as to pass through a plurality of slots 9 that are formed in the axis direction in the core 8 . Further, the magnet wire 6 is bound together with the binding thread 11 . Furthermore, impregnation is applied to the magnet wire 6 with impregnating varnish 12 in order to improve its insulation performance.
- the insulating film 10 is provided between the core 8 and the magnet wire 6 , and between the layers of the magnet wire 6 .
- Conventional impregnating varnishes used in the impregnation of the magnet wire 6 include solventless varnish, such as polyester resins that include an aromatic olefin compound, represented by styrene, as a reactive diluent; epoxy resin based solvent varnish; and epoxy resin based solventless varnish.
- solventless varnish such as polyester resins that include an aromatic olefin compound, represented by styrene, as a reactive diluent
- epoxy resin based solvent varnish an aromatic olefin compound, represented by styrene
- epoxy resin based solventless varnish epoxy resin based solventless varnish
- refrigeration and air-conditioning apparatuses conventionally use chlorofluorocarbon refrigerants such as dichlorodifluoromethane (R-12) and hydrochlorofluorocarbon refrigerants such as monochlorodifluoromethane (R-22) (hereinafter, these refrigerants are referred to as “conventional refrigerants”).
- chlorofluorocarbon refrigerants such as dichlorodifluoromethane (R-12) and hydrochlorofluorocarbon refrigerants such as monochlorodifluoromethane (R-22)
- conventional refrigerants When conventional refrigerants are used in refrigeration and air-conditioning apparatuses, mineral oil based or alkylbenzenic based refrigerating machine oil or the like (hereinafter, referred to as “conventional refrigerating machine oil”) with low polarity are typically used.
- hydrofluorocarbon refrigerants such as 1,1,1,2-tetrafluoroethane (R-134a) that does not contain any chlorine atom in its molecules (hereinafter, may also be referred to as “alternative refrigerant”) are used in refrigeration and air-conditioning apparatuses.
- Hydrofluorocarbon refrigerants are refrigerants with zero ozone depleting potential.
- alternative refrigerating machine oil based on polyalkylene glycol, ester, or ether (hereinafter, referred to as “alternative refrigerating machine oil”) that have high polarity and high compatibility with the alternative refrigerant is used.
- the cured varnish (impregnating varnish after thermal curing) in the hermetic vessel 1 is in an environment with a high-temperature high-pressure refrigerant system, the refrigerant system such as a conventional refrigerant/refrigerating machine oil, alternative refrigerant/refrigerating machine oil, or natural refrigerant/refrigerating machine oil.
- the refrigerant system such as a conventional refrigerant/refrigerating machine oil, alternative refrigerant/refrigerating machine oil, or natural refrigerant/refrigerating machine oil.
- refrigerant systems such as alternative refrigerant/alternative refrigerating machine oil and natural refrigerant/alternative refrigerating machine oil have higher polarity compared to that of the conventional refrigerant/refrigerating machine oil
- alternative refrigerant or a natural refrigerant when used in a refrigeration and air-conditioning apparatus, degradation of the cured varnish and dissolving from the cured varnish into the refrigerant system occur.
- the extractability from the cured varnish is high when CO 2 is used as the refrigerant.
- the impregnating varnish when the impregnating varnish includes components with low polarity, the compatibility between the extract that is extracted (dissolved) from the cured varnish and the refrigerating machine oil is low.
- substances with low molecular weight or the like is educed and is accumulated as sludge in an expansion unit, such as a capillary tube and an expansion valve, in the refrigeration and air-conditioning cycle, resulting in clogging of the expansion unit after operating for a long period of time.
- the impregnating varnish needs to have excellent resistance to the refrigerant system, such as little deterioration suppressing deterioration of mechanical strength, low extractability to the refrigerant system, and the like.
- an aqueous epoxy resin emulsion containing the following dissolved and/or dispersed in water: A) at least one binder selected from a group consisting of epoxy resins and modified epoxy resins; B) at least one polyurethane-based associative thickener; and C) at least one catalyst for curing that can be produced by allowing at least one boron trifluoride complex to react with at least one compound having at least one epoxy group” see, Patent Literature 1, for example.
- the known impregnating varnish disclosed in Patent Literature 1, for example aims to reduce volatile components and the like that volatiles during thermal curing.
- Patent Literature 1 Japanese Patent Publication No. 3904516 (claim 1)
- Patent Literature 1 the extraction characteristics of the cured varnish of the impregnating varnish described in Patent Literature 1 is not mentioned when in the refrigerant system such as the alternative refrigerant/refrigerating machine oil or the natural refrigerant/refrigerating machine oil. Further, in the alternative refrigerant/refrigerating machine oil refrigerant system or the natural refrigerant/refrigerating machine oil refrigerant system, the compatibility of the extract extracted from the cured varnish and the refrigerant system is not mentioned.
- the present invention has been made to solve the above-mentioned problems, and an object is to obtain water-dispersible varnish, in the alternative refrigerant/refrigerating machine oil refrigerant system or the natural refrigerant/refrigerating machine oil refrigerant system, that is capable of solving both problems, namely, reducing the volatile components and the like during thermal curing and resistance of the cured varnish to the refrigerant system. And a further object is to obtain water-dispersible varnish, an electric compressor using the water-dispersible varnish and a method of manufacturing the electric compressor, and a refrigeration and air-conditioning apparatus equipped with the electric compressor.
- the water-dispersible varnish according to the present invention that is used in an electric compressor mounted on a refrigeration and air-conditioning apparatus, which uses a refrigerant having hydrofluorocarbon as a main component or a refrigerant having natural refrigerant as a main component, and that insulates and fixes a stator of the electric compressor, the water-dispersible varnish being a mixture including at least one epoxy acrylate resin having two or more (meth) acryloyl groups in one molecule as a thermosetting resin, the epoxy acrylate resin expressed by either one of the following General Formulas (I) to (III); at least one among a vinyl monomer having an ether bond, a vinyl monomer having an ester bond, a 1-alkylvinyl monomer having an ether bond, and a 1-alkylvinyl monomer having an ester bond as a reactive diluent; an organic peroxide as a reaction initiator; and
- R 1 , R 2 , and R 3 each individually represent H or CH 3
- R 4 represents a group expressed by the following general formula:
- n represents an integer of 1 to 6 ⁇ ;
- R 6 , R 7 , and R 8 each individually represent H or CH 3
- R 9 represents a group expressed by the following general formula:
- R 10 , R 11 , and R 12 each individually represent H or CH 3
- R 13 , R 14 , and R 15 represents a group expressed by the following general formula:
- p represents an integer from 1 to 6 ⁇ .
- a method, according to the present invention, of manufacturing an electric compressor mounted on a refrigeration and air-conditioning apparatus, which uses a refrigerant having hydrofluorocarbon as a main component or a refrigerant having natural refrigerant as a main component is a method of manufacturing an electric compressor including a hermetic vessel housing a motor component and a compression component that is driven by the motor component, the hermetic vessel retaining in a bottom portion a refrigerating machine oil.
- the method includes a step of insulating and fixing a magnet wire of a stator of the motor component using the water-dispersible varnish of any one of claims 1 to 8 as impregnating varnish, and
- an electric compressor according to the invention is mounted on a refrigeration and air-conditioning apparatus, which uses a refrigerant having hydrofluorocarbon as a main component of a refrigerant having natural refrigerant as a main component, in which the electric compressor includes
- a hermetic vessel housing a motor component and a compression component that is driven by the motor component, the hermetic vessel retaining in a bottom portion a refrigerating machine oil, wherein
- the electric compressor uses the above-mentioned water-dispersible varnish as impregnating varnish insulating and fixing a magnet wire of a stator of the motor component.
- a refrigeration and air-conditioning apparatus is a refrigeration and air-conditioning apparatus that uses a refrigerant having hydrofluorocarbon as a main component or a refrigerant having natural refrigerant as a main component, and is equipped with the above-mentioned electric compressor.
- the impregnating varnish according to the invention is water-dispersible varnish, volatile components or the like during thermal curing can be reduced in the alternative refrigerant/refrigerating machine oil refrigerant system or the natural refrigerant/refrigerating machine oil refrigerant system.
- the impregnating varnish according to the invention is water-dispersible varnish that is a mixture of a specific thermosetting resin as a base polymer, a specific vinyl monomer as reactive diluent, organic peroxide as reaction initiator, and water, cured varnish exhibiting excellent resistance (little deterioration suppressing deterioration of mechanical strength, low extractability to the refrigerant system, and the like.) to the alternative refrigerant/refrigerating machine oil refrigerant system or the natural refrigerant/refrigerating machine oil refrigerant system can be obtained.
- FIG. 1 is a schematic explanatory diagram (schematic diagram of a longitudinal section) illustrating an embodiment of an electric compressor mounted on a refrigeration and air-conditioning apparatus.
- FIG. 2 is a partial schematic explanatory diagram illustrating a stator of a motor component in FIG. 1 , in which FIG. 2A is a plan view and FIG. 2B is a side view partially showing a cross sectional view.
- Water-dispersible varnish according to the embodiment uses a monomer, as its reactive diluent, that has excellent compatibility with alternative refrigerating machine oil based on polyalkylene glycol, ester, or ether. Further, this water-dispersible varnish is water-dispersible varnish having small energy loss during its hardening process and is one capable of reducing environmental load.
- One of the significant features of the embodiment is the use of the above-mentioned water-dispersible varnish for the impregnating varnish.
- an organic acid metal salt, a photoinitiator, and the like may be mixed.
- the base polymer is a thermosetting resin having two or more (meth) acryloyl groups in one molecule and is an epoxy acrylate resin (vinyl ester resin).
- This epoxy acrylate resin has low extractability in the alternative refrigerant/refrigerating machine oil refrigerant system and has excellent hydrolysis resistance.
- epoxy acrylate resin for example, there are compounds expressed by the following general formula (I).
- R 1 , R 2 , and R 3 each individually represent H or CH 3
- R 4 represents a group expressed by the following general formula:
- n represents an integer from 1 to 6 ⁇
- epoxy acrylate resin for example, there are compounds expressed by the following general formula (II).
- R 6 , R 1 , and R 8 each individually represent H or CH 3
- R 9 represents a group expressed by the following general formula:
- n represents an integer from 1 to 6 ⁇
- epoxy acrylate resin for example, there are compounds expressed by the following general formula (III).
- R 10 , R 11 , and R 12 each individually represent H or CH 3
- R 13 , R 14 , and R 15 represents a group expressed by the following general formula:
- p represents an integer from 1 to 6 ⁇
- epoxy acrylate resins may be used alone or as a mixture of two or more of the kind.
- the reactive diluent is a vinyl monomer that has excellent compatibility with the alternative refrigerating machine oil such as polyalkylene glycol oil, ester oil, ether oil, and the like. It is preferable for the vinyl monomer for the reactive diluent to be a vinyl monomer having an intramolecular ether bond, a vinyl monomer having an intramolecular ester bond, a 1-alkylvinyl monomer having an intramolecular ether bond, or a 1-alkylvinyl monomer having an intramolecular ester bond.
- vinyl monomer for example, there are compounds such as 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, lauryl (meth) acrylate, and ethoxydiethylene glycol (meth) acrylate expressed by the following general formula (IV)
- R 16 represents a hydrogen atom or an alkyl group having one to five carbon atoms
- R 17 represents —(CH 2 ) q — (q is an integer of 1 to 6) or —(CH(R 18 )O) r —
- R 18 is a hydrogen atom or an alkyl group having one to five carbon atoms, r is an integer of 1 to 6
- X represents H, OH, or OCO(R 19 )
- R 19 is an alkyl group having one to five carbon atoms, a vinyl group, or a 1-alkylvinyl group including an alkyl group having one to five carbon atoms
- vinyl monomer for example, there are compounds such as diethyleneglycol-bis-allylcarbonate expressed by the following general formula (V).
- vinyl monomers may be used alone or as a mixture of two or more of the kind.
- 2-hydroxyethyl (meth) acrylate and hydroxypropyl (meth) acrylate are preferred.
- the ratio of the thermosetting resin to the vinyl monomer for the reactive diluent is desirably 10:90 or more, and more preferably 30:70 or more.
- the ratio of the thermosetting resin to the vinyl monomer for the reactive diluent is desirably 90:10 or less, and more preferably 70:30 or less.
- a polyfunctional vinyl monomer having three or more, preferably three to 6 (meth) acryloyl groups or allyl groups in one molecule may be used as a reactive diluent, as necessary.
- polyfunctional vinyl monomer for example, there are esters or ethers that can be obtained by reaction between (A) carboxylic acid, such as trimellitic acid and pyromellitic acid, or alcohol, such as trimethylolpropane, trihydroxyethylisocyanurate, and pentaerythritol, (B) vinyl group-containing monomer, such as acrylic acid, methacrylic acid, and allyl alcohol. More preferably, as such polyfunctional vinyl monomer, trimethylolpropanetrimethacrylate, tris(2-hydroxyethyl)isocyanurate triacrylate, and dipentaerythritol hexaacrylate can be cited, by way of example.
- carboxylic acid such as trimellitic acid and pyromellitic acid
- alcohol such as trimethylolpropane, trihydroxyethylisocyanurate, and pentaerythritol
- vinyl group-containing monomer such as acrylic acid, methacrylic acid, and
- the polyfunctional vinyl monomer may be partially replaced with the vinyl monomer for the reactive diluent that has excellent compatibility with the refrigerating machine oil such as polyalkylene glycol oil, ester oil, ether oil and the like.
- the amount of the polyfunctional vinyl monomer is desirably 3 wt % or higher of the vinyl monomer for the reactive diluent, and more preferably, 20 wt % or higher thereof.
- the amount of the polyfunctional vinyl monomer is desirably 60 wt % or lower of the vinyl monomer for the reactive diluent, and more preferably, 50 wt % or lower thereof.
- the organic peroxide which is a reaction initiator used in the embodiment, is not limited to a specific organic peroxide.
- organic peroxide used as a reaction initiator perhexyl such as t-hexyl hydroperoxide, acyl peroxide such as benzoyl peroxide, peracid ester such as t-butyl peroxybenzoate, organic hydroperoxide such as tetramethylbutyl hydroperoxide, and dialkyl peroxide such as dicumyl peroxide may be preferably cited, by way of example.
- the amount of the organic peroxide is, relative to 100 parts by weight of the entire amount of the water-dispersible varnish, desirably 0.05 part by weight or higher, and more preferably, 0.3 part by weight or higher. Further, in order to eliminate the pot life characteristics of the water-dispersible varnish from becoming significantly short, the amount of the organic peroxide is, relative to 100 parts by weight of the entire amount of the water-dispersible varnish, desirably 5 parts by weight or lower, and more preferably, 3 parts by weight or lower.
- organic acid metal salt may be mixed into the water-dispersible varnish.
- organic acid metal salt in combination with the base polymer, the surface hardenability of the water-dispersible varnish will be improved significantly, and, thus, it will be possible to reduce the amount of extraction.
- organic acid metal salt salt composed of organic acid such as octylic acid, naphthenic acid, or the like, and metal such as Co, Mn, Sn, Ni, Zn, Pb, Cr, Fe, or the like may be cited, by way of example.
- organic acid metal salt cobalt naphthenate, manganese naphthenate, tin naphthenate, nickel naphthenate, zinc naphthenate, lead naphthenate, chromium naphthenate, iron naphthenate, and the like may be preferably cited, by way of example.
- the amount of the organic acid metal salt is, relative to 100 parts by weight of the entire amount of the water-dispersible varnish, desirably 0.015 part by weight or higher, and more preferably, 0.03 part by weight or higher. Further, in order to eliminate the pot life characteristics of the water-dispersible varnish from deteriorating, the amount of the organic acid metal salt is, relative to 100 parts by weight of the entire amount of the water-dispersible varnish, desirably 3 parts by weight or lower, and more preferably, 1.5 parts by weight or lower.
- a photoinitiator may be mixed into the water-dispersible varnish as a reaction initiator.
- the photoinitiator used in the embodiment is not limited to a specific photoinitiator.
- a photoinitiator benzoin ether compounds such as benzoin isobutyl ether, hydroxycyclohexyl phenyl ketone, or the like, benzyl ketal compounds such as benzil dimethylketal or the like, acetophenone derivatives such as 2-Hydroxy-2-methylpropiophenone, and ketone compounds such as 4,4′-bis(dimethylamino)benzophenone may be preferably cited, by way of example.
- the amount of the photoinitiator is, relative to 100 parts by weight of the entire amount of the water-dispersible varnish, desirably 0.2 part by weight or higher, and more preferably, 0.5 part by weight or higher. Further, in order to eliminate the risk of large amount of photoinitiator from the cured varnish to extract into the refrigerant becoming a contamination source of the refrigerant system, the amount of the photoinitiator is, relative to 100 parts by weight of the entire amount of the water-dispersible varnish, desirably 15 parts by weight or lower, and more preferably, 10 parts by weight or lower.
- a surfactant may be mixed into the water-dispersible varnish.
- the use of a surfactant will enable the coating weight to the magnet wire to be uniform.
- the surfactant used in the embodiment is a water-soluble surfactant, but the surfactant is not limited in particular.
- nonionic surfactant such as polyoxyethylene alkyl ether, polyoxyalkylene derivative, sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene sorbitol fatty acid ester, glycerine fatty acid ester, polyoxyethylene fatty acid ester, polyoxyethylene hydrogenated castor oil, polyoxyethylene alkylamine, alkyl alkanolamide; and anionic surfactants such as sodium lauryl sulfate, higher alcohol sodium sulfate, alkyl sulfate ester salt, polyoxyethylene alkyl ether sulfate ester salt, alkyl benzene sulfonate salt, sodium alkyl naphthalene sulfonate, sodium dialkyl sulfosuccinate, sodium alkyl diphenyl
- surfactants may be used alone or as a mixture of two or more of the kind.
- (poly)oxyalkylene alkenyl ether is preferred.
- This surfactant has low extractability in the refrigerant/refrigerating machine oil and has excellent hydrolysis resistance.
- the amount of the surfactant used in the embodiment is, relative to 100 parts by weight of the amount of the base polymer, desirably 0.5 part by weight or higher, and more preferably, 3 parts by weight or higher. Further, in order to eliminate the risk of becoming a cause of decrease in the heat resistance of the cured varnish, the surfactant used in the embodiment is desirably 20 parts by weight or lower, and more preferably, 15 parts by weight or lower.
- the water-dispersible varnish of the embodiment is obtained by mixing, for example, the above-mentioned organic compounds such as the thermosetting resin, the reactive diluent, the catalyst, the organic acid metal salt, the photoinitiator, the surfactant, and the like with water.
- the ratio of the organic compounds to water is desirably 15:85 or more, and more preferably, 30:70 or more.
- the ratio of the organic compounds to water is desirably 90:10 or less, and more preferably 70:30 or less.
- thermosetting resin vinyl monomer and organic peroxide for the reactive diluent, surfactant, and water
- polyfunctional vinyl monomer, organic acid metal salt, photoinitiator may be appropriately adjusted and mixed.
- a method of manufacturing a hermetic electric compressor according to the embodiment will be described.
- the hermetic electric compressor illustrated in FIGS. 1 and 2 is manufactured.
- One of the significant features of the method of manufacturing the hermetic electric compressor according to the embodiment is the use of the above water-dispersible varnish as an impregnating varnish to insulate and fix a magnet wire 6 of a stator 21 of a motor component 2 .
- the water-dispersible varnish After impregnating the magnet wire 6 of the stator 21 of the motor component 2 with the water-dispersible varnish, the water-dispersible varnish is heated at a specific temperature for a specific period of time and is cured. Such stator is incorporated to obtain the hermetic electric compressor.
- heating temperature is 130 degrees C. or higher (preferably 140 degrees C. or higher) and 180 degrees C. or lower (preferably 175 degrees C. or lower); and the heating period of time is 0.5 hours or more (preferably 1 hour or more) and 5 hours or less (preferably 4 hours or less).
- the heating temperature and the heating period of time are under the lower limit values, there will be an uncured portion in the water-dispersible varnish during the curing process, and various electrical and mechanical characteristics will drop. Further, if the heating temperature and the heating period of time exceed the upper limit values, the crosslinking reaction during the curing process will be unbalanced and will be the cause of crack in the insulated product (cured varnish).
- the water-dispersible varnish according to the embodiment will be further described in detail. Note that the water-dispersible varnish according to the embodiment is not limited to the below examples.
- Impregnating varnish water-dispersible varnish was obtained by mixing 25 parts by weight of epoxy acrylate (bisphenol A type, two acryloyl groups in one molecule, number average molecular weight of approximately 500) as base polymer; 12 parts by weight of 2-hydroxypropyl methacrylate and 10 parts by weight of 2-hydroxypropyl acrylate as reactive diluent; 0.5 part by weight of t-butyl peroxybenzoate as organic peroxide; 0.05 part by weight of cobalt naphthenate as organic acid metal salt; 3 parts by weight of surfactant; and 50 parts by weight of water.
- epoxy acrylate bisphenol A type, two acryloyl groups in one molecule, number average molecular weight of approximately 500
- a sheet was fabricated by enclosing the obtained impregnating varnish between glass plates with a gap of 0.2 mm therebetween, thermal curing at 160 degrees C. for 3 hours, and removing from the glass plates.
- Extractability (%) (weight of the flask of the extraction apparatus after evaporation of methanol ⁇ weight of the flask of the extraction apparatus before the test)/the weight of the sheet before the test ⁇ 100.
- a flow reduction rate of a throttled portion of an expansion valve of the simulated refrigeration cycle was measured.
- the flow reduction rate of the throttled portion of the expansion valve was calculated by sending refrigerant or air with a constant pressure (0.49N/m 2 ) into the piping and measuring the flow rate at the outlet, and by obtaining the ratio between the flow rate at the outlet before the 2000-hour operation and that after the operation.
- the appearance change of the expansion valve and the pipeline was visually checked after the 2000-hour accelerated reliability test was run. An inspection was carried out based on the evaluation criteria below. Note that the check on the appearance change of the expansion valve and the pipeline was carried out by disassembling the simulated refrigeration cycle and the real machine and visually checking the inner surfaces and the like of the expansion valve and the pipeline.
- Example 1 Using impregnating varnish obtained in the same manner as Example 1, a sheet was fabricated by thermal curing at 170 degrees C. for 2 hours. Other fabricating conditions of the sheet are the same as those of Example 1.
- Example 1 Using impregnating varnish obtained in the same manner as Example 1, a sheet was fabricated by thermal curing at 130 degrees C. for 5 hours. Other fabricating conditions of the sheet are the same as those of Example 1.
- Example 1 Using impregnating varnish obtained in the same manner as Example 1, a sheet was fabricated by thermal curing at 150 degrees C. for 5 hours. Other fabricating conditions of the sheet are the same as those of Example 1.
- Example 2 Using impregnating varnish obtained in the same manner as Example 1, a sheet was fabricated by thermal curing at 180 degrees C. for 0.5 hours. Other fabricating conditions of the sheet are the same as those of Example 1.
- Impregnating varnish water-dispersible varnish was obtained by mixing 30 parts by weight of epoxy acrylate (novolac type, two acryloyl groups in one molecule, number average molecular weight of approximately 850) as base polymer; 27 parts by weight of 2-hydroxyethyl methacrylate and 10 parts by weight of trimethylolpropanetrimethacrylate as reactive diluent; 0.5 part by weight of t-butyl peroxybenzoate as organic peroxide; 0.05 part by weight of cobalt naphthenate as organic acid metal salt; 3 parts by weight of surfactant; and 40 parts by weight of water.
- epoxy acrylate novolac type, two acryloyl groups in one molecule, number average molecular weight of approximately 850
- 2-hydroxyethyl methacrylate and 10 parts by weight of trimethylolpropanetrimethacrylate as reactive diluent
- t-butyl peroxybenzoate as organic peroxide
- Example 6 using the impregnating varnish that was obtained in Example 6, a real machine (the hermetic electric compressor shown in FIGS. 1 and 2 ) was fabricated by the same conditions as Example 1.
- Example 6 Using impregnating varnish obtained in the same manner as Example 6, a sheet was fabricated by thermal curing at 145 degrees C. for 2 hours. Other fabricating conditions of the sheet are the same as those of Example 6.
- Example 6 Using impregnating varnish obtained in the same manner as Example 6, a sheet was fabricated by thermal curing at 170 degrees C. for 3.5 hours. Other fabricating conditions of the sheet are the same as those of Example 6.
- Example 6 Using impregnating varnish obtained in the same manner as Example 6, a sheet was fabricated by thermal curing at 150 degrees C. for 3 hours. Other fabricating conditions of the sheet are the same as those of Example 6.
- Example 6 Using impregnating varnish obtained in the same manner as Example 6, a sheet was fabricated by thermal curing at 180 degrees C. for 2 hours. Other fabricating conditions of the sheet are the same as those of Example 6.
- Impregnating varnish water-dispersible varnish was obtained by mixing 20 parts by weight of unsaturated polyester resin (number average molecular weight of approximately 3500) as base polymer; 30 parts by weight of styrene as reactive diluent; 0.03 part by weight of t-butyl peroxybenzoate as organic peroxide; 0.05 part by weight of cobalt naphthenate as organic acid metal salt; 3 parts by weight of surfactant; and 50 parts by weight of water.
- unsaturated polyester resin number average molecular weight of approximately 3500
- a sheet was fabricated using this impregnating varnish by thermal curing at 160 degrees C. for 2 hours. Other fabricating conditions of the sheet are the same as those of Example 1.
- Impregnating varnish water-dispersible varnish was obtained by mixing 30 parts by weight of epoxy acrylate (bisphenol A type, two acryloyl groups in one molecule, number average molecular weight of approximately 500) as base polymer; 10 parts by weight of 2-hydroxyethyl methacrylate and 15 parts by weight of trimethyloipropanetrimethacrylate as reactive diluent; 0.5 part by weight of t-butyl peroxybenzoate as organic peroxide; 0.05 part by weight of cobalt naphthenate as organic acid metal salt; 5 parts by weight of surfactant; and 40 parts by weight of water.
- epoxy acrylate bisphenol A type, two acryloyl groups in one molecule, number average molecular weight of approximately 500
- a sheet was fabricated using this impregnating varnish by thermal curing at 190 degrees C. for 3 hours. Other fabricating conditions of the sheet are the same as those of Example 1.
- Impregnating varnish water-dispersible varnish was obtained by mixing 5 parts by weight of epoxy acrylate (novolac type, two acryloyl groups in one molecule, number average molecular weight of approximately 850) as base polymer; 37 parts by weight of 2-hydroxyethyl methacrylate and 15 parts by weight of trimethylolpropanetrimethacrylate as reactive diluent; 0.5 part by weight of t-butyl peroxybenzoate as organic peroxide; 0.05 part by weight of cobalt naphthenate as organic acid metal salt; 3 parts by weight of surfactant; and 40 parts by weight of water.
- epoxy acrylate novolac type, two acryloyl groups in one molecule, number average molecular weight of approximately 850
- base polymer 37 parts by weight of 2-hydroxyethyl methacrylate and 15 parts by weight of trimethylolpropanetrimethacrylate as reactive diluent
- t-butyl peroxybenzoate as organic peroxid
- a sheet was fabricated using this impregnating varnish by thermal curing at 155 degrees C. for 3 hours. Other fabricating conditions of the sheet are the same as those of Example 1.
- Impregnating varnish water-dispersible varnish was obtained by mixing 47 parts by weight of epoxy acrylate (bisphenol A type, two acryloyl groups in one molecule, number average molecular weight of approximately 600) as base polymer; 2 parts by weight of 2-hydroxyethyl methacrylate as reactive diluent; 0.5 part by weight of t-butyl peroxybenzoate as organic peroxide; 0.05 part by weight of cobalt naphthenate as organic acid metal salt; 1 parts by weight of surfactant; and 50 parts by weight of water.
- epoxy acrylate bisphenol A type, two acryloyl groups in one molecule, number average molecular weight of approximately 600
- 2-hydroxyethyl methacrylate as reactive diluent
- t-butyl peroxybenzoate as organic peroxide
- cobalt naphthenate as organic acid metal salt
- surfactant 1 parts by weight of surfactant
- Impregnating varnish water-dispersible varnish was obtained by mixing 5 parts by weight of epoxy acrylate (novolac type, two acryloyl groups in one molecule, number average molecular weight of approximately 850) as base polymer; 3 parts by weight of 2-hydroxyethyl methacrylate and 2 parts by weight of trimethylolpropanetrimethacrylate as reactive diluent; 0.5 part by weight of t-butyl peroxybenzoate as organic peroxide; 0.05 part by weight of cobalt naphthenate as organic acid metal salt; 3 parts by weight of surfactant; and 87 parts by weight of water.
- epoxy acrylate novolac type, two acryloyl groups in one molecule, number average molecular weight of approximately 850
- 2-hydroxyethyl methacrylate and 2 parts by weight of trimethylolpropanetrimethacrylate as reactive diluent
- t-butyl peroxybenzoate as organic peroxide
- a sheet was fabricated using this impregnating varnish by thermal curing at 155 degrees C. for 3 hours. Other fabricating conditions of the sheet are the same as those of Example 1.
- Impregnating varnish water-dispersible varnish was obtained by mixing 50 parts by weight of epoxy acrylate (novolac type, two acryloyl groups in one molecule, number average molecular weight of approximately 600) as base polymer; 25 parts by weight of 2-hydroxyethyl methacrylate and 20 parts by weight of trimethyloipropanetrimethacrylate as reactive diluent; 0.5 part by weight of t-butyl peroxybenzoate as organic peroxide; 0.05 part by weight of cobalt naphthenate as organic acid metal salt; 1 parts by weight of surfactant; and 4 parts by weight of water.
- epoxy acrylate novolac type, two acryloyl groups in one molecule, number average molecular weight of approximately 600
- base polymer 25 parts by weight of 2-hydroxyethyl methacrylate and 20 parts by weight of trimethyloipropanetrimethacrylate as reactive diluent
- t-butyl peroxybenzoate as organic peroxide
- a sheet was fabricated using this impregnating varnish by thermal curing at 160 degrees C. for 3 hours. Other fabricating conditions of the sheet are the same as those of Example 1.
- Impregnating varnish water-dispersible varnish was obtained by mixing 25 parts by weight of epoxy acrylate (novolac type, two acryloyl groups in one molecule, number average molecular weight of approximately 400) as base polymer; 20 parts by weight of 2-hydroxyethyl methacrylate and 15 parts by weight of trimethylolpropanetrimethacrylate as reactive diluent; 0.5 part by weight of t-butyl peroxybenzoate as organic peroxide; 0.05 part by weight of cobalt naphthenate as organic acid metal salt; 25 parts by weight of surfactant; and 15 parts by weight of water.
- epoxy acrylate novolac type, two acryloyl groups in one molecule, number average molecular weight of approximately 400
- 2-hydroxyethyl methacrylate and 15 parts by weight of trimethylolpropanetrimethacrylate as reactive diluent
- t-butyl peroxybenzoate as organic peroxide
- a sheet was fabricated using this impregnating varnish by thermal curing at 160 degrees C. for 3 hours. Other fabricating conditions of the sheet are the same as those of Example 1.
- the impregnating varnish according to the invention is a water-dispersible type, volatile components or the like during thermal curing can be reduced in the alternative refrigerant/refrigerating machine oil refrigerant system or the natural refrigerant/refrigerating machine oil refrigerant system.
- the impregnating varnish is a water-dispersible type that is a mixture of a specific thermosetting resin as a base polymer, a specific vinyl monomer as reactive diluent, organic peroxide as reaction initiator, and water, cured varnish exhibiting excellent resistance (little deterioration suppressing deterioration of mechanical strength, low extractability to the refrigerant system, low eduction from the refrigerant system, and the like.) to the alternative refrigerant/refrigerating machine oil refrigerant system or the natural refrigerant/refrigerating machine oil refrigerant system can be obtained.
- a hermetic electric compressor having a magnet wire 6 that is insulated and fixed by the cured varnish having the above advantages can be obtained, and a refrigeration and air-conditioning apparatus equipped with this compressor can be obtained. Therefore, an electric compressor that is capable of suppressing clogging of the capillary tube, expansion valve, and the like can be obtained, and a refrigeration and air-conditioning apparatus equipped with this compressor can be obtained.
- water-dispersible varnish according to the embodiment is not limited to hermetic electric compressors, and it goes without saying that, it can be used in semi-hermetic electric compressors and the like.
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- Emergency Medicine (AREA)
- Physics & Mathematics (AREA)
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- General Engineering & Computer Science (AREA)
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- Insulation, Fastening Of Motor, Generator Windings (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Abstract
Description
{where R1, R2, and R3 each individually represent H or CH3, and R4 represents a group expressed by the following general formula:
{where R6, R7, and R8 each individually represent H or CH3, and R9 represents a group expressed by the following general formula:
{where R10, R11, and R12 each individually represent H or CH3, and R13, R14, and R15 represents a group expressed by the following general formula:
- (A) a thermosetting resin that is a epoxy acrylate resin having two or more (meth) acryloyl groups in one molecule (hereinafter, also referred to as “base polymer”);
- (B) as a reactive diluent having excellent compatibility with refrigerating machine oil based on polyalkylene glycol, ester, or ether, a vinyl monomer having an ether bond, a vinyl monomer having an ester bond, a 1-alkylvinyl monomer having an ether bond, or a 1-alkylvinyl monomer having an ester bond (hereinafter, these vinyl monomers and 1-alkylvinyl monomers are also collectively referred to as “vinyl monomer for reactive diluent”);
- (C) an organic peroxide as a reaction initiator; and
- (D) water.
- (E) a polyfunctional vinyl monomer having three or more (meth) acryloyl groups or an allyl group in one molecule,
- (F) an organic peroxide as a reaction initiator; and
- (G) a water-soluble organic compound as a surfactant may be mixed into the above-described water-dispersible varnish.
{where R1, R2, and R3 each individually represent H or CH3, and R4 represents a group expressed by the following general formula:
{where R6, R1, and R8 each individually represent H or CH3, and R9 represents a group expressed by the following general formula:
{where R10, R11, and R12 each individually represent H or CH3, and R13, R14, and R15 represents a group expressed by the following general formula:
{where R16 represents a hydrogen atom or an alkyl group having one to five carbon atoms, R17 represents —(CH2)q— (q is an integer of 1 to 6) or —(CH(R18)O)r— (R18 is a hydrogen atom or an alkyl group having one to five carbon atoms, r is an integer of 1 to 6), and X represents H, OH, or OCO(R19) (R19 is an alkyl group having one to five carbon atoms, a vinyl group, or a 1-alkylvinyl group including an alkyl group having one to five carbon atoms)}
H2C═CH—CH2—OR20 (v)
(where R20 represents a hydrogen atom or a group expressed by the following formula.)
Extractability (%)=(weight of the flask of the extraction apparatus after evaporation of methanol−weight of the flask of the extraction apparatus before the test)/the weight of the sheet before the test×100.
Flow reduction rate (%)=(outlet flow rate after the 2000-hour operation/outlet flow rate before the 2000-hour operation)×100.
TABLE 1 | |||
Rate of extraction (%) | Rate of extraction (%) | ||
when using varnish | when using varnish | ||
before storage | stored for 1-month | ||
Example | ||
1 | 0.2 | 0.2 |
2 | 0.4 | 0.4 |
3 | 0.3 | 0.3 |
4 | 0.3 | 0.3 |
5 | 0.2 | 0.2 |
6 | 0.3 | 0.3 |
7 | 0.4 | 0.4 |
8 | 0.4 | 0.4 |
9 | 0.5 | 0.5 |
10 | 0.4 | 0.4 |
Comparative | ||
Example | ||
1 | 3.5 | 4.3 |
2 | Not measurable | Not measurable |
3 | 4.3 | 5.2 |
4 | 6.8 | 9.3 |
5 | Not measurable | Not measurable |
6 | 5.9 | 8.5 |
7 | Not measurable | Not measurable |
8 | Not measurable | Not measurable |
9 | 7.6 | 16.3 |
10 | 6.9 | 12.6 |
TABLE 2 | ||
Results of accelerated | ||
reliability test |
Flow reduc- | ||||
tion rate at | Visual | |||
a throttled | inspec- | |||
Refrigerant and Refrigerant oil | portion (%) | tion | ||
Example | |||
1 | R-407C and Ester oil | 98 | ∘ |
2 | CO2 and Polyalkylene glycol | 97 | ∘ |
3 | R-290 and Polyvinyl ether | 97 | ∘ |
4 | R-1270 and Polyalkylene glycol | 99 | ∘ |
5 | Ammonia and Polyvinyl ether | 96 | ∘ |
6 | R-407C and Paraffinic mineral | 98 | ∘ |
oil + alkylbenzene-based |
|||
7 | CO2 and Polyvinyl ether | 98 | ∘ |
8 | R-290 and Polyalkylene glycol | 99 | ∘ |
9 | R-1270 and Polyvinyl ether | 98 | ∘ |
10 | Ammonia and Polyalkylene | 97 | ∘ |
glycol | |||
Comparative | |||
Example | |||
1 | R-407C and Ester oil | 87 | |
2 | CO2 and Polyvinyl ether | Not evaluable | x |
3 | R-290 and Polyalkylene glycol | 89 | x |
4 | R-1270 and Polyalkylene glycol | 86 | |
5 | Ammonia and Polyvinyl ether | Not evaluable | x |
6 | R-407C and Paraffinic mineral | 88 | Δ |
oil + alkylbenzene-based |
|||
7 | CO2 and Polyalkylene glycol | Not evaluable | x |
8 | R-290 and Polyvinyl ether | Not evaluable | x |
9 | R-1270 and Polyvinyl ether | 86 | |
10 | Ammonia and Polyalkylene | 88 | x |
glycol | |||
Claims (18)
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PCT/JP2009/063745 WO2011016103A1 (en) | 2009-08-03 | 2009-08-03 | Water dispersible varnish, motor compressor using the water dispersible varnish, method for manufacturing the motor compressor, and refrigerator/air conditioner equipped with the motor compressor |
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US20120189768A1 US20120189768A1 (en) | 2012-07-26 |
US8912274B2 true US8912274B2 (en) | 2014-12-16 |
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US (1) | US8912274B2 (en) |
JP (1) | JP5528453B2 (en) |
KR (1) | KR101302823B1 (en) |
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JP6037363B2 (en) * | 2013-10-16 | 2016-12-07 | 三菱電機株式会社 | Water-dispersed insulating varnish composition, insulating coil using the same, and method for producing hermetic electric compressor |
DE102013017147A1 (en) * | 2013-10-16 | 2015-04-16 | Gea Refrigeration Germany Gmbh | compressor |
US11155730B2 (en) * | 2015-10-08 | 2021-10-26 | Mitsubishi Electric Corporation | Solvent-free varnish composition, insulated coil, process for producing same, rotating machine, and closed electric compressor |
CN106749985B (en) * | 2016-11-24 | 2019-07-09 | 苏州吉人高新材料股份有限公司 | A kind of composite emulsion and preparation method thereof based on epoxy modified acrylic resin |
JPWO2019221178A1 (en) * | 2018-05-18 | 2021-07-08 | ダイキン工業株式会社 | Refrigeration cycle equipment |
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2009
- 2009-08-03 KR KR1020127003045A patent/KR101302823B1/en active IP Right Grant
- 2009-08-03 WO PCT/JP2009/063745 patent/WO2011016103A1/en active Application Filing
- 2009-08-03 JP JP2011525703A patent/JP5528453B2/en active Active
- 2009-08-03 CN CN200980160763XA patent/CN102471429B/en active Active
- 2009-08-03 US US13/388,910 patent/US8912274B2/en active Active
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JP5528453B2 (en) | 2014-06-25 |
JPWO2011016103A1 (en) | 2013-01-10 |
US20120189768A1 (en) | 2012-07-26 |
CN102471429A (en) | 2012-05-23 |
CN102471429B (en) | 2013-08-21 |
KR101302823B1 (en) | 2013-09-02 |
WO2011016103A1 (en) | 2011-02-10 |
KR20120052958A (en) | 2012-05-24 |
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